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2-Dicyclohexylphosphino-2'-(N,N-Dimethylamino)Biphenyl

    • Product Name 2-Dicyclohexylphosphino-2'-(N,N-Dimethylamino)Biphenyl
    • Alias SPhos
    • Einecs 811-930-0
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    719317

    Chemical Name 2-Dicyclohexylphosphino-2'-(N,N-Dimethylamino)biphenyl
    Cas Number 911407-16-8
    Molecular Formula C26H40NP
    Molecular Weight 397.58
    Appearance White to off-white solid
    Purity Typically >98%
    Solubility Soluble in organic solvents (e.g., toluene, THF, dichloromethane)
    Melting Point 75-80°C (approximate)
    Boiling Point Decomposes before boiling
    Storage Conditions Under inert atmosphere, away from air and moisture
    Smiles CN(C)c1ccccc1-c1ccccc1P(C2CCCCC2)C3CCCCC3
    Synonyms SPhos-NMe2, DCYP-NMe2
    Hazard Statements May cause skin or eye irritation

    As an accredited 2-Dicyclohexylphosphino-2'-(N,N-Dimethylamino)Biphenyl factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 1-gram quantity of 2-Dicyclohexylphosphino-2'-(N,N-Dimethylamino)Biphenyl is sealed in an amber glass vial, under inert gas.
    Shipping 2-Dicyclohexylphosphino-2'-(N,N-Dimethylamino)biphenyl is shipped in sealed containers under inert atmosphere, such as nitrogen or argon, to prevent air and moisture exposure. Packaging meets regulations for hazardous chemical transportation. During transit, the product is protected from heat, direct sunlight, vibration, and physical damage to ensure safe delivery.
    Storage 2-Dicyclohexylphosphino-2'-(N,N-Dimethylamino)biphenyl should be stored under an inert atmosphere (such as nitrogen or argon) in a tightly sealed container. Store it in a cool, dry, and well-ventilated area, away from moisture, air, and oxidizing agents. Exposure to air and light should be minimized to prevent degradation. Handle using proper protective equipment and follow standard laboratory safety protocols.
    Application of 2-Dicyclohexylphosphino-2'-(N,N-Dimethylamino)Biphenyl

    Applications of 2-Dicyclohexylphosphino-2'-(N,N-Dimethylamino)Biphenyl in Industrial Manufacturing

    As a specialized manufacturer, we supply 2-Dicyclohexylphosphino-2'-(N,N-Dimethylamino)Biphenyl to major chemical industries worldwide. Our customers use this advanced phosphine ligand in processes requiring high selectivity, excellent catalytic activity, and reliable scalability. Below, we outline key industrial application segments, compliance pathways, practical usage ratios, technical integration into downstream manufacturing, and real-world finished product output.

    1. Pharmaceutical Fine Chemical Synthesis Catalysis

    Palladium-catalyzed cross-coupling reactions in pharmaceutical R&D and commercial API production rely on this ligand to control reaction specificity and minimize by-product formation. Leading process chemists incorporate this compound in Suzuki-Miyaura, Buchwald-Hartwig, and related coupling methodologies for regulated drug intermediates. The ligand’s steric and electronic profile supports routes requiring tight control over aryl-aryl or aryl-amine bond formation, aligning with strict cGMP manufacturing quality and patient safety.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 211 Current Good Manufacturing Practice for Finished Pharmaceuticals
    • EU GMP Directive 2003/94/EC
    • Japanese Pharmaceutical Affairs Law (JPAL)

    Typical usage ratio

    • 0.5–3.0 mol% relative to palladium; adjusted according to substrate and scale-up batch optimization

    Downstream process integration

    • Added to reactor during catalyst charge phase of coupling steps; may require glovebox or inert atmosphere for nutrient-sensitive syntheses

    Final product types

    • Regulated pharmaceutical intermediates
    • Small molecule APIs
    • Complex heterocyclic scaffolds for oncology and CNS drugs
    • Advanced patent-protected substances moving toward late-stage clinical trials

    2. Electronic Materials: OLED and Semiconductor Precursor Manufacturing

    Global electronics manufacturers turn to this phosphine ligand as a core component in palladium-mediated C–N and C–C bond formations used to prepare high-purity organic semiconductors and device precursors. Its role in enabling high-yield, low-impurity coupling supports fabrication of materials for OLED displays, photovoltaic devices, and organic FETs, where even minor catalyst residue or side-products degrade device performance or reliability. The ligand’s structure allows precise control over electronic material purity at the multi-kilogram scale.

    Industry compliance standards

    • IEC 61249-2-21 Halogen-Free Environmental Standard (for electronic components)
    • RoHS Directive 2011/65/EU Restriction of Hazardous Substances
    • ISO 9001:2015 Quality Management Systems (semiconductor materials)

    Typical usage ratio

    • 0.2–2.5 mol% to the palladium source in aryl cross-coupling; optimized by polymer molecular weight and target purity level

    Downstream process integration

    • Loaded as ligand component in catalyst solution during assembly-line synthesis of monomers and polymeric semiconductor backbones; strict monitoring via HPLC/ICP for trace contaminants

    Final product types

    • OLED emitter and host materials
    • P-type and N-type organic semiconductors
    • Organic photovoltaic (OPV) precursor chemicals
    • Photoresist and imaging material intermediates

    3. Agrochemical Active Ingredient and Intermediate Synthesis

    Major agrochemical companies and contract manufacturers deploy this phosphine ligand in the synthesis of complex herbicide, fungicide, and insecticide building blocks, especially those requiring high-purity C-aryl or C-heteroaryl motifs. It offers reduced catalyst loadings, low batch-to-batch variation, and scalability from pilot plant to commercial production. The ligand helps minimize unwanted side reactions, supporting compliance with food safety and environmental standards globally.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products (JMPS)
    • EU REACH Regulation (EC) No 1907/2006
    • EPA 40 CFR Part 158 (Pesticide Data Requirements)
    • ISO 17025 (Analytical Laboratory Accreditation for Quality Control)

    Typical usage ratio

    • 0.7–2.0 mol% as ligand component per 1 mol% palladium; adapted for substrate reactivity and process economics across kilo and ton scale runs

    Downstream process integration

    • Direct addition into batch or flow reactors during coupling, typically after charge of halide and boronic/amine components; ligand scavenged in post-reaction purification to ensure regulatory thresholds

    Final product types

    • Technical grade pesticide intermediates
    • Crystalline agrochemical actives (post-purification)
    • Seed treatment fungicide molecules
    • Environmental metabolite reference standards

    4. Specialty Polymer and High-Performance Resin Production

    This ligand enables advanced cross-coupling polymerization reactions essential for synthesizing specialty resins, engineering plastics, and functionalized polymer materials. Resin and polymer manufacturers rely on this component for precise molecular structure control—crucial in automotive, aerospace, and high-end industrial coatings. Its use allows for efficiently constructing backbones with controlled branching or specialty end-group insertion, tuning polymer property profiles to demanding user specifications.

    Industry compliance standards

    • ISO 9001:2015 for Quality Management Systems in Polymer Manufacturing
    • REACH Regulation (EC) No. 1907/2006 for specialty chemicals
    • ASTM D638 and D256 Mechanical Testing Standards for Polymers
    • Automotive OEM material approval specifications (e.g., VW TL 52640)

    Typical usage ratio

    • 0.2–1.5 mol% phosphine ligand relative to palladium; tuned according to desired polymer molecular weight and branching density

    Downstream process integration

    • Weigh and add ligand solution in initial polymerization charge with monomers and catalyst; inert nitrogen purging adopted during critical addition steps to suppress unwanted side reactions

    Final product types

    • Polyarylenes for advanced composites
    • Thermostable resins for electronic encapsulation
    • Functionalized engineering plastics
    • Polymer adhesives for aerospace and electronics
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